| [1] |
Zeng Y Q, Zhao J, Wang S F, Wang W J, Lu Y R, Xi S B, Xu W, Yoda Y, Masuda R, Li X N, Huang Y Q, Liu B, Zhang T. Unraveling the dynamic low-spin state evolution of single-Fe-atom sites for efficient CO2 electroreduction[J]. J. Am. Chem. Soc., 2025, 147(46): 42539-42548. https://doi.org/10.1021/jacs.5c13466.
|
| [2] |
Francke R, Schille B, Roemelt M. Homogeneously catalyzed electroreduction of carbon dioxide—methods, mechanisms, and catalysts[J]. Chem. Rev., 2018, 118(9): 4631-4701. https://doi.org/10.1021/acs.chemrev.7b00459.
doi: 10.1021/acs.chemrev.7b00459
URL
pmid: 29319300
|
| [3] |
Jin S, Hao Z M, Zhang K, Yan Z H, Chen J. Advances and challenges for the electrochemical reduction of CO2 to CO: from fundamentals to industrialization[J]. Angew. Chem. Int. Ed., 2021, 60(38): 20627-20648. https://doi.org/10.1002/anie.202101818.
doi: 10.1002/anie.v60.38
URL
|
| [4] |
Boutin E, Merakeb L, Ma B, Boudy B, Wang M, Bonin J, Anxolabéhère-Mallart E, Robert M. Molecular catalysis of CO2 reduction: recent advances and perspectives in electrochemical and light-driven processes with selected Fe, Ni and Co aza macrocyclic and polypyridine complexes[J]. Chem. Soc. Rev., 2020, 49(16): 5772-5809. https://doi.org/10.1039/D0CS00218F.
doi: 10.1039/D0CS00218F
URL
|
| [5] |
Kortlever R, Shen J, Schouten K J P, Calle-Vallejo F, Koper M T M. Catalysts and reaction pathways for the electrochemical reduction of carbon dioxide[J]. J. Phys. Chem. Lett., 2015, 6(20): 4073-4082. https://doi.org/10.1021/acs.jpclett.5b01559.
doi: 10.1021/acs.jpclett.5b01559
URL
pmid: 26722779
|
| [6] |
Su D J, Xiang S Q, Gao S T, Jiang Y M, Liu X H, Zhang W, Zhao L B, Tian Z Q. Kinetic understanding of catalytic selectivity and product distribution of electrochemical carbon dioxide reduction reaction[J]. JACS Au, 2023, 3(3): 905-918. https://doi.org/10.1021/jacsau.3c00002.
doi: 10.1021/jacsau.3c00002
URL
|
| [7] |
Saha P, Amanullah S, Dey A. Selectivity in electrochemical CO2 reduction[J]. Acc. Chem. Res., 2022, 55(2): 134-144. https://doi.org/10.1021/acs.accounts.1c00678.
doi: 10.1021/acs.accounts.1c00678
URL
|
| [8] |
Xue Y Y, Zhang L J, Kuang M, Zheng G F. Tuning the CO2 and CO electroreduction by rate-determining and selectivity-determining steps[J]. ACS Appl. Mater. Interfaces, 2025, 17(8): 11375-11388. https://doi.org/10.1021/acsami.4c21239.
doi: 10.1021/acsami.4c21239
URL
|
| [9] |
Lin Y X, Wang S C, Liu H J, Liu X, Yang L, Su X Z, Shan L, Li X Y, Song L. Regulating the electrocatalytic active centers for accelerated proton transfer towards efficient CO2 reduction[J]. Natl. Sci. Rev., 2025, 12(3): nwaf010. https://doi.org/10.1093/nsr/nwaf010.
|
| [10] |
Wang H, Ma C Q, Lu Q P, Gu M Z, Jiang L, Hao Y X, Hu F, Li L L, Wang G F, Peng S J, Zhang X J. Precise tuning of functional group spatial distribution on porphyrin rings for enhanced CO2 electroreduction selectivity[J]. Angew. Chem. Int. Ed., 2025, 64(19): e202501091. https://doi.org/10.1002/anie.202501091.
doi: 10.1002/anie.v64.19
URL
|
| [11] |
Wang Y, Ma F Y, Zhang P F, Zhang G Q, Zhao Z H, Zheng X B, Zhao H, Zhang J W, Dong Y M, Zhu Y F. Tuning *CO-*CHO dimerization via twisted electron localization of asymmetrically coordinated Cu-Cu dual sites by P and N scatterings boosts CO2 electroreduction[J]. ACS Catal., 2025, 15(21): 17703-17714. https://doi.org/10.1021/acscatal.5c04995.
doi: 10.1021/acscatal.5c04995
URL
|
| [12] |
Xiong L, Zhan S Q, Di Ciano L, Li S S, Liu R M, Lu S J, Yao P, Fu X B, Yue Q. Elucidating the donor/acceptor regulatory mechanism for CO2 electroreduction[J]. Adv. Mater., 2025, e12478. https://doi.org/10.1002/adma.202512478.
|
| [13] |
Liu N, Pham T M, Han Y N, Yang L F, Bokareva O S, Bartling S, Springer A, Spannenberg A, Kubis C, Weiss J, Doronkin D E, Ju W, Francke R. Heterogenized copper(II) phenanthroline catalysts for electroreduction of CO2 to C2 compounds: substitution on the ligand causes structural changes to the molecular framework and stability enhancement[J]. Adv. Mater., 2025, 38(3): e13702. https://doi.org/10.1002/adma.202513702.
doi: 10.1002/adma.v38.3
URL
|
| [14] |
Yang Z W, Chen J M, Qiu L Q, Xie W J, He L N. Molecular engineering of metal complexes for electrocatalytic carbon dioxide reduction: from adjustment of intrinsic activity to molecular immobilization[J]. Angew. Chem. Int. Ed., 2022, 61(44): e202205301. https://doi.org/10.1002/anie.202205301.
doi: 10.1002/anie.v61.44
URL
|
| [15] |
Kong X D, Zhu J C, Xu Z F, Geng Z G. Fundamentals and challenges of ligand modification in heterogeneous electrocatalysis[J]. Angew. Chem. Int. Ed., 2025, 64(1): e202417562. https://doi.org/10.1002/anie.202417562.
doi: 10.1002/anie.v64.1
URL
|
| [16] |
Zhang D A, Liu X, Zhao Y, Zhang H, Rudnev A V, Li J F. In situ Raman spectroscopic studies of CO2 reduction reactions: from catalyst surface structures to reaction mechanisms[J]. Chem. Sci., 2025, 16(12): 4916-4936. https://doi.org/10.1039/D5SC00569H.
doi: 10.1039/D5SC00569H
URL
|
| [17] |
Li X D, Wang S M, Li L, Sun Y F, Xie Y. Progress and perspective for in situ studies of CO2 reduction[J]. J. Am. Chem. Soc., 2020, 142(21): 9567-9581. https://doi.org/10.1021/jacs.0c02973.
|
| [18] |
Ren X Y, Zhao J, Li X N, Shao J M, Pan B B, Salamé A, Boutin E, Groizard T, Wang S F, Ding J, Zhang X, Huang W Y, Zeng W J, Liu C Y, Li Y G, Hung S F, Huang Y Q, Robert M, Liu B. In-situ spectroscopic probe of the intrinsic structure feature of single-atom center in electrochemical CO/CO2 reduction to methanol[J]. Nat. Commun., 2023, 14(1): 3401. https://doi.org/10.1038/s41467-023-39153-6.
doi: 10.1038/s41467-023-39153-6
URL
|
| [19] |
Sakamoto N, Sekizawa K, Shirai S, Nonaka T, Arai T, Sato S, Morikawa T. Dinuclear Cu(I) molecular electrocatalyst for CO2-to-C3 product conversion[J]. Nat. Catal., 2024, 7(5): 574-584. https://doi.org/10.1038/s41929-024-01147-y.
doi: 10.1038/s41929-024-01147-y
URL
|
| [20] |
Wu M J, Yang S Y, Gao Y, Chen Z S, Dong F, Lei H Y, Yang Y K, Chen N, Omanovic S, Regier T, Cui X, Xia B Y, Zhang G X, Sun S H. Steering CO2 electroreduction pathway via tuning microenvironment of cobalt center in molecular catalysts[J]. ACS Nano, 2025, 19(36): 32507-32517. https://doi.org/10.1021/acsnano.5c09554.
doi: 10.1021/acsnano.5c09554
URL
|
| [21] |
Yang H Z, Guo N, Xi S B, Wu Y, Yao B Q, He Q, Zhang C, Wang L. Potential-driven structural distortion in cobalt phthalocyanine for electrocatalytic CO2/CO reduction towards methanol[J]. Nat. Commun., 2024, 15(1): 7703. https://doi.org/10.1038/s41467-024-52168-x.
doi: 10.1038/s41467-024-52168-x
URL
|
| [22] |
Ogawa S, Yamaguchi T, Gotoh N. Preparation of a conjugated tautomer of 1,14:7,8-diethenotetrapyrido-[2,1,6-de:2',1',6'-gh:2'',1'',6''-kl:2''',1''',6'''-na][1,3,5,8,10,12]hexa-azacyclotetradecine and its metal derivatives[J]. J. Chem. Soc., Perkin Trans. 1, 1974: 976-978. https://doi.org/10.1039/P19740000976.
|
| [23] |
Jiang Y, Jung H, Joo S H, Sun Q K, Li C Q, Noh H J, Oh I, Kim Y J, Kwak S K, Yoo J W, Baek J B. Catalyst- and solvent-free synthesis of a chemically stable aza-bridged bis(phenanthroline) macrocycle-linked covalent organic framework[J]. Angew. Chem. Int. Ed., 2021, 60(31): 17191-17197. https://doi.org/10.1002/anie.202106389.
doi: 10.1002/anie.202106389
URL
pmid: 34114283
|
| [24] |
Hennig H, Benedix R, Hempel K, Reinhold J. Zur Konstitution von Bis-(phenanthrolin)-kobalt(II)-Komplexen[J]. Z. Anorg. Allg. Chem., 1975, 412(2): 141-147. https://doi.org/10.1002/zaac.19754120206.
doi: 10.1002/zaac.v412:2
URL
|
| [25] |
Isaacs M, Canales J C, Riquelme A, Lucero M, Aguirre M J, Costamagna J. Contribution of the ligand to the electroreduction of CO2 catalyzed by a cobalt(II) macrocyclic complex[J]. J. Coord. Chem., 2003, 56(14): 1193-1201. https://doi.org/10.1080/00958970310001624447.
doi: 10.1080/00958970310001624447
URL
|
| [26] |
Chen X J, Ren H, Peng W, Zhang H M, Lu J T, Zhuang L. Highly efficient molecular cobalt electrode for (photo)electrochemical hydrogen evolution[J]. J. Phys. Chem. C, 2014, 118(36): 20791-20798. https://doi.org/10.1021/jp5061792.
doi: 10.1021/jp5061792
URL
|
| [27] |
Zhang X, Wu Z S, Zhang X, Li L W, Li Y Y, Xu H M, Li X X, Yu X L, Zhang Z S, Liang Y Y, Wang H L. Highly selective and active CO2 reduction electrocatalysts based on cobalt phthalocyanine/carbon nanotube hybrid structures[J]. Nat. Commun., 2017, 8(1): 14675. https://doi.org/10.1038/ncomms14675.
doi: 10.1038/ncomms14675
URL
|
| [28] |
Zhu Q S, Rooney C L, Shema H, Zeng C, Panetier J A, Gross E, Wang H L, Baker L R. The solvation environment of molecularly dispersed cobalt phthalocyanine determines methanol selectivity during electrocatalytic CO2 reduction[J]. Nat. Catal., 2024, 7(9): 987-999. https://doi.org/10.1038/s41929-024-01190-9.
doi: 10.1038/s41929-024-01190-9
URL
|
| [29] |
Rohrbach D F, Heineman W R, Deutsch E. Thin-layer spectroelectrochemical studies of cobalt and copper Schiff base complexes[J]. Inorg. Chem., 1979, 18(9): 2536-2542. https://doi.org/10.1021/ic50199a041.
doi: 10.1021/ic50199a041
URL
|
| [30] |
Chen J X, Wang X Y, Cui X, Li Y Y, Feng Y Q, Wei Z W. In situ probing and identification of electrochemical reaction intermediates by floating electrolytic electrospray mass spectrometry[J]. Angew. Chem. Int. Ed., 2023, 62(12): e202219302. https://doi.org/10.1002/anie.202219302.
doi: 10.1002/anie.v62.12
URL
|
| [31] |
Zhao K, Pang W Y, Jiang S Y, Hu C Y, Liu P R, Cui D D, An X F, Tian B J, Gao C, Zhang P, Tian M, Fu D, Zhao H J. Operando reconstruction-induced CO2 reduction activity and selectivity for cobalt-based photocatalysis[J]. Nano Res., 2023, 16(4): 4812-4820. https://doi.org/10.1007/s12274-023-5432-5.
doi: 10.1007/s12274-023-5432-5
URL
|
| [32] |
Wu F, Jiang F S, Yang J H, Dai W Y, Lan D H, Shen J, Fang Z J. Investigation of molecular mechanism of cobalt porphyrin catalyzed CO2 electrochemical reduction in ionic liquid by in-situ SERS[J]. Molecules, 2023, 28(6): 2747. https://doi.org/10.3390/molecules28062747.
doi: 10.3390/molecules28062747
URL
|
| [33] |
Jia J Z, Zhao X H, Hu W H, Wang Y T, Huang J F, Huang J, Li H, Peng Y, Ma H Y, Xu C L. Role of cobalt phthalocyanine on the formation of high-valent cobalt species revealed by in situ Raman spectroscopy[J]. J. Mater. Chem. A, 2023, 11(15): 8141-8149. https://doi.org/10.1039/D2TA10063K.
doi: 10.1039/D2TA10063K
URL
|